HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620747Generated: October 30, 2026
Isopropenyl acetate → HCID 15926017, compound
https://huagongshe.com/reaction/620747
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropenyl acetate | HCID 7916 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | Methoxytri-n-butylstannane | HCID 11964040 | — |
| Reactant | 6-Bromo-3-methyl[1,3]oxazolo[4,5-b]pyridin-2(3H)-one | HCID 15926016 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 15926017 | HCID 15926017 | — |
Reaction Steps
3-Methyl-6-bromo-oxazolo[4,5-b]pyridin-2(3H)-one (2.58 g) (0.012 mole) in 80 ml of benzene is treated with 365 mg tri-o-tolylphosphine, 138 mg palladium acetate, 1.87 g (0.018 mole) of isopropenyl acetate and 5.9 g (0.18 mole) of tributyltin methoxide. This is sealed in a high pressure tube and heated to 70° C. for 25 hours. The reaction mixture is then quenched with 20 ml sat. ammonium chloride and diluted with 50 ml ethyl acetate. The organic phase separates, dried over sodium sulfate and concentrated to dryness. The residue is dissolved in methylene chloride, washed with sat. KF solution, filtered through a cotton plug, dried over sodium sulfate and concentrated to dryness to obtain crude product. This is chromatographed using 200×60 mm SiO2, EtOAc (100%) as eluent. The desired product is identified by NMR and used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04822794 |
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| Source dataset | uspto-grants-1989_04 |
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| ORD ID | ord-1f654ca4b47d4298876afea062cc4995 |
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| Source note | uspto-grants-1989_04 |
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